| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:81680806-81681003 | Common:1; Rare:50 | ||||
| chr16:83717843-83718048 | Common:2; Rare:51 | ||||
| chr16:85136906-85137164 | Rare:62 | ||||
| chr16:85151807-85151948 | Common:1; Rare:31 | ||||
| chr16:85312844-85313080 | Common:3; Rare:47 | ||||
| chr16:86157794-86158127 | Common:3; Rare:86 | ||||
| chr16:86195942-86196378 | Common:1; Rare:108 | ||||
| chr16:86198603-86198905 | Common:2; Rare:73 | ||||
| chr16:86768374-86768629 | Common:2; Rare:71 | ||||
| chr16:86868228-86868396 | Common:3; Rare:45 | ||||
| chr16:87822708-87822899 | Common:4; Rare:50 | ||||
| chr16:89344029-89344318 | Rare:77 | ||||
| chr16:89542763-89543049 | Common:7; Rare:83 | ||||
| chr17:4708608-4708808 | Common:6; Rare:67 | ||||
| chr17:4945969-4946262 | Common:5; Rare:100; Clinvar (benign):1; Clinvar (pathogenic):1 |